1-{(2R,4S,5R)-4-Hydroxy-5-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-2-yl}-4-(4-nitro-phenoxy)-1H-pyrimidin-2-one

Base Information

• Chemical Name: 1-{(2R,4S,5R)-4-Hydroxy-5-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-2-yl}-4-(4-nitro-phenoxy)-1H-pyrimidin-2-one
• CAS No.: 1053694-40-8
• Molecular Formula: C₃₅H₃₁N₃O₈
• Molecular Weight: 621.646
• Mol file: 1053694-40-8.mol

Synonyms:

Chemical Property of 1-{(2R,4S,5R)-4-Hydroxy-5-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-2-yl}-4-(4-nitro-phenoxy)-1H-pyrimidin-2-one

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1-{(2R,4S,5R)-4-Hydroxy-5-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-2-yl}-4-(4-nitro-phenoxy)-1H-pyrimidin-2-one

There total 1 articles about 1-{(2R,4S,5R)-4-Hydroxy-5-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-2-yl}-4-(4-nitro-phenoxy)-1H-pyrimidin-2-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

4-(p-nitrophenoxy)-1-(β-D-2-deoxyribofuranosyl)pyrimidin-2(1H)-one (189005-86-5) + mono-4-methoxytrityl chloride (14470-28-1) → 1-{(2R,4S,5R)-4-Hydroxy-5-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-2-yl}-4-(4-nitro-phenoxy)-1H-pyrimidin-2-one (1053694-40-8)

Guidance literature:

With pyridine; cooling;

DOI:10.1039/b403652b

Reference yield:

1-{(2R,4S,5R)-4-Hydroxy-5-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-2-yl}-4-(4-nitro-phenoxy)-1H-pyrimidin-2-one (1053694-40-8) → N4-[2-(2,2,2-trifluoroacetamido)ethyl]-5'-O-(4-methoxytrityl)-2'-deoxycytidine 3'-H-phosphonate

Guidance literature:

Multi-step reaction with 3 steps

1.1: 0.93 g / ethanol / 2 h

2.1: 97 percent / ethanol / 1 h / 0 °C

3.1: imidazole; PCl₃; triethylamine / CH₂Cl₂ / 1 h / -78 °C

3.2: 92 percent / aq. TEAB / CH₂Cl₂ / pH 7.5

With 1H-imidazole; triethylamine; phosphorus trichloride; In ethanol; dichloromethane;

DOI:10.1039/b403652b

Reference yield:

1-{(2R,4S,5R)-4-Hydroxy-5-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-2-yl}-4-(4-nitro-phenoxy)-1H-pyrimidin-2-one (1053694-40-8) → N4-[2-(2,2,2-trifluoroacetamido)ethyl]-5'-O-(4-methoxytrityl)-2'-deoxycytidine (745062-93-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 0.93 g / ethanol / 2 h

2: 97 percent / ethanol / 1 h / 0 °C

In ethanol;

DOI:10.1039/b403652b

upstream raw materials:

4-(p-nitrophenoxy)-1-(β-D-2-deoxyribofuranosyl)pyrimidin-2(1H)-one

mono-4-methoxytrityl chloride

Downstream raw materials:

N⁴-(2-aminoethyl)-5'-O-(4-monomethoxytrityl)-2'-deoxycytidine

N⁴-[2-(2,2,2-trifluoroacetamido)ethyl]-5'-O-(4-methoxytrityl)-2'-deoxycytidine